20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition.

Piton, Amélie

20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition. [electronic resource] - European journal of human genetics : EJHG Jun 2014 - 776-83 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1476-5438

10.1038/ejhg.2013.243 doi


Amino Acid Sequence
Attention Deficit and Disruptive Behavior Disorders--genetics
Base Sequence
Child Development Disorders, Pervasive--genetics
Family Health
Female
Genetic Predisposition to Disease--genetics
High-Throughput Nucleotide Sequencing--methods
Humans
Intellectual Disability--genetics
Male
Models, Molecular
Monoamine Oxidase--chemistry
Mutation, Missense
Pedigree
Protein Structure, Tertiary